Cephalexin - 65862-018-40 - (Cephalexin)

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Drug Information of Cephalexin

Product NDC: 65862-018
Proprietary Name: Cephalexin
Non Proprietary Name: Cephalexin
Active Ingredient(s): 250    mg/1 & nbsp;   Cephalexin
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Cephalexin

Product NDC: 65862-018
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065253
Marketing Category: ANDA
Start Marketing Date: 20051116

Package Information of Cephalexin

Package NDC: 65862-018-40
Package Description: 40 CAPSULE in 1 BOTTLE (65862-018-40)

NDC Information of Cephalexin

NDC Code 65862-018-40
Proprietary Name Cephalexin
Package Description 40 CAPSULE in 1 BOTTLE (65862-018-40)
Product NDC 65862-018
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cephalexin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20051116
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name CEPHALEXIN
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cephalexin


General Information